Lichen Sclerosus: Any other women dealing with this disease?
Is anyone out there dealing with this disease? I am currently using a compound ointment that my oncologist prescribed but I'm looking for possible lazer treatments or anything else that might now be available.
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I wash every 24-48 hours then reapply after washing. You may find you need to apply differently.
I had to use clobestol ountment. It helped but is very painful. Hope you feel better.
Hello,
I use Green Tea Extract, no alcohol. I leave it on for 24 to 48 hrs. Then wash and reapply. It’s helpful to have a routine that suits you. No worries …I sincerely hope it help you.
Thank you I really appreciate you sharing your routine. I bought green tea extract (Organic Matcha Powder), and Organic Neem Oil from the Health shop today, so going to give it a go!
I just recently noticed some vaginal burning after urinating, so on day 4 decided to take a look. I saw a raw-looking spot on inner labia, so went to women's clinic. The advanced nurse that I saw felt the need to do a biopsy on the spot, even though I had wanted to take a more wait-and-see approach, since it was only day 4. Long story short, I got a call from someone at this clinic who said your biopsy says "lichen." Steroid cream has been called in.
That's it. They hung up. There was no mention of a follow-up appointment to discuss aftercare or anything.
Today is three weeks since the biopsy, and the wound is not fully closed up. I did not have stitches, just the silver nitrate. So, I'm a bit concerned about whether the skin of the wound should have a hole or not. I made myself a follow-up appointment to see the nurse who did the biopsy; couldn't get in with a physician in a timely manner.
So, I have a couple of other concerns. One is that I've been putting the clobetasol cream on the open wound and wonder how it affects the healing process of the actual wound caused by the punch biopsy. Two is that I requested a copy of the pathology report of the biopsy, so I could read it for myself, since the clinic didn't tell me much when they called.
The pathology report says "chronic, lichenoid vulvitis without atypia additional stain for fungal organisms is negative. Sections show a punch biopsy of reactive vulvar squamous mucosa in which there is an intense, lichenoid type chronic inflammatory reaction with an associated spongiotic interface pattern. The chronic inflammatory reaction consistent of plymorphous lymphocytes which dissipate toward the lower aspects of the submucosa. Scattered intraepithelial small lymphocytes are present. There is no obvious squamous atypia or viral cytopathic features. Additional immunostains were performed with appropriate controls. There is a predominance of T-scells do not appear to show an aberrant, phenotype on evaluation of CD3, CD4, CD5, CD7, and cd8. Rare B-cells are noted by CD20. Fungal organisms are not identified on GMS special stain evaluation. The findings are likely nonspecific but exclusion of a possible clinical history of lichen planus is suggested."
It's that last sentence that gets me. Nonspecific????
When this clinic called me, they made no mention of a follow-up appointment to discuss the findings whatsoever. I have since called the clinic to make an appointment to see if my biopsy wound is healing properly, and I plan to ask at this time what is the recommended treatment plan, besides them just phoning in clobetasol cream that says apply twice a day for 2 weeks.
I no longer burn when I pee. And the raw spot I once had, is now a punch biopsy wound, so not sure how the spot would've progressed had it not been punched. Wondering if I should try to find a vulvar specialist or a dermatologist.
@murphyt
Welcome to Mayo Connect. I am sure you have read the other comments and realize you are not alone with concerns about Lichen Sclerosus.
I was diagnosed about 4 years ago, and similar to you, they did a punch biopsy to confirm. I am not sure if I ever read the pathology report. Once healed, the biopsy site just looks like a white spot. I am glad you are following up to see if things are healing.
In my case, I will need to use the clobetasol cream long term, not just during a flare up. During a flare up, the provider had me use more often and then once flare up is done I use multiple times a week.
After my initial flare up, I had appointment to recheck in 6 months. Now I see a provider in gynecology once a year to make sure everything looks OK.
It is very important to get the flare up under control and monitor in future so does not get worse.
Definitely ask about ongoing monitoring and maybe make an appointment for 6 months out with provider to recheck.
I have had lichen for around 50 years.
A number of years ago. I had a major flare. The doctor I saw told me to start using cotton toilet paper. It help me.
Just a thought.
Wish you the best.
I've had lichen sclerosus for five years. Diagnosed by punch biopsy. I read that taking Evening Primrose Oil helps. And a suggestion from my Gyn at the time to install a bidet. They have all sorts of units, ones that mount on existing toilets or even units that replace your toilet. But those 2 things have helped me and visiting my Gyn to keep a check on the tissues. It seems to be working for me. Best of luck to you.
Yes, my experience is a vulvar specialist is helpful if you can find one. Just to note that lichen planus and lichen schlerosa are not the same disorder. I've had LS for many years and was always treated with chlobetesal, but you will need specific advice on how to use it to minimize risks and how often to be checked for side effects or disorder progression. Some women go into remission and can use alternative vulvar treatments. Hope this happens for you!
@minnesota10 - Cotton toilet paper?? Which brands make cotton toilet paper?